Pediatric Surgical Speciality
30 Years of Clinical Practice
Dr. Ramesh Santhanakrishnan, a senior Pediatric Surgeon with nearly 30 years of clinical practice in Bangalore.
☑️ Specialized Pediatric Care: Focuses on advanced pediatric surgery and medical services.
☑️ Experienced Team: Led by Dr. Ramesh Santhanakrishnan with over 30 years of experience.
☑️ Comprehensive Services: Includes Pediatric Surgery, Urology, Neurology, ENT, Gastroenterology, and more.
☑️ Compassionate Care: Committed to providing ethical, child-friendly treatment.
☑️ Modern Facilities: Equipped with state-of-the-art medical equipment for pediatric needs.
A Sneek Peak into our Clinic
Why Choose Our Pediatric Speciality Services
☑️ Three decade long legacy
☑️ Best-in-class tools and technology to deliver advanced pediatric surgical services
☑️ Brought thousands of children out of Pediatric conditions enabling them to live a happy and healthy life
☑️ Being empathetic and humane are integral to our approach
☑️ We relentlessly pursue our passion for excellence
Services Offered: Pediatric Surgical Super Specialities
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Frequently Asked Questions (FAQs)
A pediatrician is a medical doctor who specializes in the care of children. Pediatricians have undergone special training in the health and illnesses of infants, teens and young adults.
In the five year course leading to the basic medical degree, paediatrics is only a small part. To specialise in children’s disorders (that has a course different from an adult) it takes an
additional three years. Pediatricians specialize in the physical, emotional, and social health of
children from birth to young adulthood. Children deserve to be examined by someone who has
studied their health and disease separately and gained expertise in them.
Some of the ley criteria in choosing the right pediatrician for your child are: Qualification and
Experience of the Doctor; Ethos and Values of the Doctor; Tools, Technology and Equipments
used; Proximity and Availability; Social Proof/Testimonials from Patients and Parents.
Your child should not only see the pediatrician for an illness. It is also important to schedule
well-child-care exams regularly, beginning in infancy. Also called well-care visits or checkups,
these routine examinations provide the best opportunity for the doctor to observe the progress
of your child's physical and mental growth and development; to counsel and teach parents; to
detect problems through screening tests; to provide immunizations, and to get to know one
another.We recommend the following schedule for routine well-care visits:
3 to 5 days; 1 month; 2 months; 4 months; 6 months; 9 months; 12 months; 15 months; 18
months; 2 years; 2 1/2 years; 3 years; 4 years; 5 years; And every year thereafter for an annual
health supervision visit that includes a physical exam as well as a developmental, behavioral,
and learning assessment.
Our Clinic is open 5 PM – 7 PM Monday – Friday.
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Top Pediatric Genetics Doctors in Bangalore – Expert Care for Genetic Conditions in Children
Seeking the best paediatric genetics doctor in Bangalore? Our city’s most experienced and skilled kids’ geneticists provide compassionate care to children with hereditary and genetic issues. Our NABH-accredited hospitals offer around-the-clock services by experts experienced in medical genetics, genetic testing, and counseling, as well as working closely with other pediatric divisions such as paediatricians, counselors, and others to help your child.
Gain access to world-renowned pediatric genetics specialists focusing on early diagnosis, personalized treatment, and ongoing care for rare and complex diseases.
What is Pediatric Genetics and Why Is It Important?
The field of pediatric genetics is a medical specialty that concerns itself with diagnosing, managing, and counselling individuals with genetic disorders. These disorders can impact your child’s development, metabolism, growth, or overall health and commonly appear at birth or during childhood.
What is a Pediatric Geneticist?
A pediatric geneticist is a physician who specializes in evaluating children suspected or known to have genetic disorders. They work closely with families to determine the underlying mechanisms for developmental delays, congenital disabilities, metabolic problems, and other inherited conditions. These physicians also help families with child genetic testing, providing personalized insights through DNA analysis and clinical interpretation.
Consultation with a pediatric geneticist is essential early on. Early diagnosis of genetic cases can enable targeted interventions, avoid complications, and allow families to make an informed choice for therapeutic management and future reproductive planning. With top-of-the-line early diagnosis and world-class care, pediatric genetics makes a difference in the lives of children born with genetic conditions on their journey to a healthy future.
What Does a Pediatric Genetics Doctor Do?
A pediatric genetics doctor, or medical geneticist for children, plays a vital role in identifying and managing a wide range of pediatric genetic disorders.
These doctors provide a family-centered approach to care, addressing the child’s immediate health needs and the long-term effects of health conditions on the child’s everyday life.
Diagnosis of Rare Genetic and Hereditary Disorders
An essential professional duty of the pediatric geneticist is the correct diagnosis of complex, frequently uncommon genetic disorders. Advanced child genetic testing methods, such as chromosomal analysis, whole-exome sequencing, or enzyme assays, can uncover abnormalities associated with delays, metabolic disorders, and congenital anomalies.
Genetic Counseling for a Family
Genetic counseling to families is a major aspect of their work. This will also include discussing how the genetic disorder is inherited, the risk of recurrence in a future pregnancy, and testing available to other family members. Pediatric genetic counseling provides families with the information they need to make decisions, as well as emotional support while they prepare for long-term care
Individualised Care & Long-Term Management
Pediatric geneticists work with other experts to create personalized treatment plans after a diagnosis. These interventions are therapies, such as medications, diets, or mechanical interventions, that may be helpful in various ways. The care of the child with a hereditary disorder is lifelong, and ongoing management is required to ensure the child reaches their potential in learning and well-being.
Integrated Meet Coordination & Monitoring
Pecists frequently collaborate with other specialists—for example, neurologists, cardiologists, endocrinologists, and developmental pediatricians—to provide comprehensive care. Regular supervision is necessary to monitor a child’s development, modify treatments, and anticipate complications.
Conditions Treated by Pediatric Geneticists
Pediatric genetics encompasses diagnosing and managing rare inherited disorders affecting a child’s growth, development, and general health. These can be anything from junior high school textbook apparent genetic congenital disabilities to more subtle chromosomal aberrations in children that only see the light of day in the form of developmental delay, or metabolic problems.
Birth Defects
Some children have textbook-clear effects, which could indicate an underlying genetic problem. Pediatric geneticists frequently diagnose and manage:
Cleft lip and palate
Clubfoot
Congenital heart defects
It is essential to ascertain whether these are primary conditions or part of a syndrome to help summarise best practice recommendations for management and counselling.
Genetic Syndromes
Children with distinctive facial features and medical problems have genetic syndromes. Common examples include:
Down syndrome
mg/d in girls affected by Turner syndrome.
Marfan syndrome (which affects connective tissue and heart function)
Pediatric geneticists assist with confirming these diagnoses through karyotyping and DNA testing and counsel the families on long-term care plans.
IEM (Inborn Errors of Metabolism)
Pediatric metabolic disorders are inherited conditions that do not allow the body to process specific substances properly. Some of these can be life‑threatening and require dietary or enzyme therapy. Conditions include:
Cystic fibrosis
through (PKU)
Tay-Sachs disease
Prevent Life-Threatening Complications. Early detection through newborn screening or child genetic testing can prevent life-threatening complications.
Developmental Disorders
Many paediatric developmental genetics consultations are prompted by unexplained speech, motor, or learning delays. Genetic testing may identify the causes of:
ASD (Autism spectrum disorder)
SpManytellectual disabilities
Such findings are helpful for the design of early intervention therapies and developmental support programs.
Hereditary Disorders
Some children are born with genetic mutations that make them susceptible to lifelong conditions or serious diseases. You may remember that children are affected by inherited diseases more broadly and in different areas, some of which include:
Hemophilia (an uncommon bleeding disease)
progressive muscle weakness (Duchenne muscular dystrophy)
Hereditary cancer syndromes (such as hereditary retinoblastoma or Li-Fraumeni syndrome)
When expert genetic analysis becomes available, families are provided with proactive screening plans and can even choose to undergo carrier testing or prenatal diagnosis.
From chromosomal anomalies in children to rare inherited ailments, pediatric geneticists offer clarity and support, and tangible direction for the path ahead, whatever that path may look like.
Pediatric Genetic Testing: What Parents Should Know
Genetic testing for kids is essential for correctly identifying conditions with unknown causes, uncovering inherited conditions early on, and guiding families through informed medical choices. If your child has features of developmental delays in the early years or physical features suggestive of congenital anomalies, or if you have a family history or a personal history of genetic illness, your pediatrician may refer your family to a pediatric genetics doctor for evaluation and testing.
What is Genetic Testing in Children?
Pediatric genetic testing is a type of genetic test done to look at a child’s DNA to see if any changes (also called mutations) can cause health problems. The tests are performed on blood, saliva, or tissue samples and are safe, noninvasive, and highly accurate.
The Types of Genetic Tests Your Child Might Get
To help identify an underlying genetic cause of your child’s symptoms, a pediatric medical geneticist may suggest one or more of the following in-depth clinical evaluations and tests:
Karyotyping: Looks for larger chromosomal problems, including missing or extra chromosomes (Down’s syndrome, for example).
CGH Array (Comparative Genomic Hybridization): This can identify missing or extra portions of chromosomes.
Whole Exome Sequencing (WES): A more comprehensive test that reads all genes’ protein-coding parts (exons) to identify rare mutations.
Enzyme Assay: Assesses the activity of a particular enzyme and helps diagnose pediatric metabolic diseases.
Non-Invasive Prenatal Testing (NIPT): This would only apply during pregnancy, but it could be relevant if your child is born with suspected genetic abnormalities.
When and Why Should I Get Tested?
Whether there is a family history of a genetic condition or not, the specifics of the genetic condition and the exact genetic mutation or mutation(s) identified in the affected family members: Are utilized to drive the genetic testing in the child.
Multiple congenital disabilities
Do I have a Developmental delay or Intellectual disability for no reason?
Metabolic issues/assets or failure to thrive
The earlier the diagnosis is made, the more personalized treatment can be and the better the prognosis. Potential preventive therapies exist for both siblings and the not-yet-born sibling.
Are Genetic Tests Safe for Children?
Yes. The vast majority of genetic tests require only a straightforward blood draw (child DNA testing) or saliva sample. There are no side effects, and the procedure is relatively painless except for slight discomfort from the blood draw.
Interpretation and Result Time Frames
The results may be available in 2 to 6 weeks, depending on the complexity of the test. Your paediatric geneticist can interpret the results for you and what they mean for your child’s health and management.
What Does a Genetic Test Cost?
Genetic testing in Bangalore would vary from ₹5,000 to ₹50,000+, depending on complexity and lab services.
(Always check with your doctor for personal recommendations and costs.)
If you’re wondering what kind of doctor tests genetics, a board-certified pediatric genetics doctor or a medical geneticist is there to walk your child’s diagnosis and care journey with expertise and empathy.
Genetic Counseling for Families
It can be a daunting and emotional diagnosis for families when a child is diagnosed with a genetic condition. Pediatric genetic counseling is a guiding hand and resource in our challenging journey. With an empathetic, teaching-based approach, genetic counselors and pediatric geneticists can support parents in understanding what they need to know to decide the best course for their child’s health and future.
Decoding Patterns of Inheritance
One of the main purposes of the family genetics conference is to simplify the difficult explanations of inheritance patterns. Parents learn how conditions are inherited — dominant? recessive? X-linked? — and what that may mean for current and future children. This information is important for determining recurrence risks and for family planning.
Planning for Future Pregnancies
In families with a history of genetic diseases, genetic risk assessment in children can estimate the possibility of genetic diseases. Couples thinking of having additional offspring become candidates for prenatal screening, preimplantation genetic diagnosis (PGD), or carrier testing, thus enabling them to make informed reproductive decisions.
For Psychosocial Needs
Being told that one’s child has a diagnosis of a lifelong genetic condition has the potential to affect the emotional health of parents and siblings. Genetic counselors offer more than just medical facts; they provide emotional support and often connect families to support groups, community resources, and therapy when needed.
Long-Term Family Support
Children with complex genetic conditions often need lifelong special care, and the same usually goes for the people who care for them. Pediatric genetic counseling gives families the tools they need to grow, adjust, and manage through these challenges with milestones and positive experiences.
By applying clinical expertise with compassion, family genetics providers can be that rock for families who receive rare or hard-to-understand diagnoses.
Pediatric Genetics Services in Bangalore – Hospitals & Clinics
Searching for a reliable paediatric genetics doctor in Bangalore? The city has some of India’s leading medical centres, providing state-of-the-art diagnostics, counseling, and treatment for children with genetic or inherited conditions. Whether you reside in Whitefield, Hebbal, Jayanagar, or Old Airport Road, you can avail of specialized care near your home.
Best Pediatric Genetic Clinics in Bangalore
Rainbow Children’s Hospital – Marathahalli & Hebbal
Rainbow is a NABH-accredited facility known for our pediatric genetics clinic in Bangalore . With a multidisciplinary group of pediatric geneticists, neonatologists, and counselors, they provide:
Sequencing the whole genome
Prenatal counseling
Prescription of Inborn Error of Metabolism
Neonatal Intensive Care Unit Support for Infants with Genetic Defects
Manipal Hospital – Old Airport Road & Kodihalli
The Pediatric Genetics & Metabolic Medicine department at Manipal is a referral center for cases of complex genetics. Services include:
Genomic diagnostics (karyotyping, WES)
Family risk assessments
Rare inherited treatments
Coordination of endocrinology and neurology for children
Aster CMI Hospital – Hebbal
Children’s genetic testing at Aster CMI has state-of-the-art facilities. Their coordinated care model consists of:
Metabolic enzyme investigation
Referrals of children to neurology, cardiology, and gastroenterology
Family genetic counseling and surveillance
Apollo Hospitals—Jayanagar & Bannerghatta
Standard of Care in Personalized Genetic Assessment. Their services cover:
Child DNA testing
Counseling for genetic causes of cancer and syndromes
Carrier testing and prenatal testing
Bangalore Baptist Hospital – Hebbal
Baptist Hospital provides an affordable kids’ genetic testing center for poor kids in Bangalore, especially for underprivileged ones. Known for:
Developmental screening in pediatrics
AND cognitive disorder assessments
Family counseling with a heart
Services Provided:
Genetic clinical testing and molecular testing in DNA
Advanced testing through partnership with the house and external lab partners
NICU support of neonates with possible genetic disease
Counseling in the preconception and prenatal period
Whether you need a geneticist near me for children or require help with a complex condition, the best hospitals in Bangalore can deliver holistic, specialized care, and even when needed, empathetic assistance for your child.
Notable Pediatric Geneticists in Bangalore
Getting connected is the first step to the correct diagnosis, care plan, and long-term support. Finding the best pediatric geneticist in Bangalore. Below is the list of Experienced Pediatric geneticist doctors in Bangalore by area, their experience, and standard availability at the hospitals.
Dr. Sridevi Hegde – Manipal Hospital
Dr. Sridevi Hegde is the best child genetic doctor in Bangalore and is currently the head of the Pediatric Genetics and Metabolic Medicine unit in Manipal Hospital. She specializes in:
Genetic syndromes and chromosomal disorders that are not common
Inborn errors of metabolism in childhood.
Prenatal Consequences and Genetic Risk Counseling
Dr Hegde has several national and international publications and is highly regarded in academic genetics.
Dr. Madhuri Maganthi – Bangalore Baptist Hospital
Dr. Madhuri, with her compassionate demeanor, specializes in:
Pediatric neurogenetics & developmental delay assessments
Genetic testing that low-income communities can afford
Counseling for other congenital and hereditary diseases
She works in outreach and training for pediatric genetics care within the community in urban and rural areas.
Dr. Mallikarjun Patil – Aster CMI Hospital
Dr.Patil is a senior pediatric genetics doctor in Bangalore who has clinical genetics and pediatrics training. His expertise includes:
Diagnosis of inborn errors of metabolism based on enzymatic assays
NICU and PICU consultations for presumed genetic diseases
Trio Whole Exome and Chromosomal Microarray, also known as chromosomal microarray analysis (CMA).
Dr. Sharat Honnatti – Vita Family Clinic
Dr. Sharat [Honnatti] is an internal medicine physician interested in genetics. He provides:
Family testing for a disease that runs in a family
Rare syndromes, Genetic counseling, and 2nd opinions
Genetic risk estimation in lifestyle
Dr. Ananya Das – Manipal Hospital
Dr. Ananya specializes in:
Pediatric endocrinology and inborn errors of metabolism.
Genetic conditions resulting from growth hormone-related problems
Syndromes of congenital origin with multisystemic
These most qualified child genetic specialists in Bangalore are dedicated to providing your family with the best pediatric genetics care, using the latest testing and counseling services.
When Should You See a Pediatric Geneticist?
Initial assessment by a pediatric geneticist may be key to finding an underlying condition, including those that are not readily apparent. If your child has any of the following signs and symptoms or a family history of a genetic condition, it’s best to consult a pediatric genetic doctor in Bangalore.
Common reasons for seeing a pediatric geneticist:
Delay with no known reason
Your child is not meeting milestones in speech, motor skills, or cognitive development.
Mental Retardation or Learning Problems
Particularly when other medical or environmental influences do not account for it.
Genetic history in the family members
Like Down syndrome, cystic fibrosis, muscular dystrophy, or inherited cancers.
Congenital disabilities
If there is a genetic component, such as heart abnormalities, cleft palate, or limb deformities.
Inborn errors of metabolism
Symptoms such as faltering growth, vomiting, seizures, or CKU.
Multiple miscarriages or the death of a baby in the family
Telling you about any chromosomal or inherited conditions.
Newborn screen results that are out of range
Any abnormal state-mandated newborn testing panels.
Abnormal physical features or growth patterns
Such as facial features, or being taller or shorter than usual.
Getting to a pediatric geneticist promptly can mean early diagnosis, intervention, and improved long-term outcomes. These specialists provide genetic testing for children and thorough counseling for families facing intricate diagnoses.
How to Choose the Right Pediatric Geneticist
Selecting a child genetic doctor is a critical step that can influence your child’s diagnosis and ongoing management. The following are some important points one should consider before choosing a pediatric geneticist in Bangalore :
Experience & Specialization
Find a physician with special training in pediatric or medical genetics and who is board-certified in either area. Expertise in complex rare syndromes, metabolic disorders, and developmental disorders is required.
Hospital Affiliation
Choose to go with geneticists linked to reputed pediatric genetics hospitals in the area, like Manipal, Aster CMI, Apollo, and Rainbow Children’s Hospital. These centres provide secondary and tertiary level diagnostics, NICU care, and multidisciplinary teams.
Multidisciplinary Team
Our team includes the expertise of long-term care professionals, and we work with a wide range of other health care professionals to provide a breadth of experience and perspective.
Accessibility & Reviews
Look up online reviews and testimonials to assess patient satisfaction. Ease of reaching for follow-ups and tele-consultation is crucial to care, particularly for families that are out-of-state in Bangalore.
For specialist pediatric genetics consultation in Bangalore, search for clinical expertise, patient-centered care, and strong institutional support. The correct physician can guide you through complex diagnoses with clarity and compassion.
Why Trust Us? – Expertise, Ethics & Excellence in Pediatric Genetic Care
When it comes to your child’s health, trust is everything. Our experienced paediatric genetics doctors in Bangalore combine years of experience, compassionate care, and state-of-the-art diagnostics to ensure your child receives nothing but the best.
Expert Team with Proven History.
Our pediatric geneticists are graduates of premier national and international institutions and are board-certified in clinical genetics and pediatrics. Many of them are associated with top hospitals such as Manipal Hospital, Aster CMI, Apollo, and Rainbow Children’s Hospital—the former three have obtained NABH accreditation for patient safety and quality care.
Advanced Technology & Diagnostics
We use the latest testing from Whole Exome Sequencing, CGH array, and metabolic panels supported by international labs and world-class infrastructure, with a precise, gold standard diagnosis at the earliest work-up.
Ethical, Family-Centered Care
All consultations are based on empathy and honesty. Through discussions and long-term planning, we help families make wise choices, utilizing the highest ethical standards in pediatrics.
Academic Engagement & Research
Our physicians are involved in genetics research, publish in medical journals, and mentor future geneticists to help keep their expertise current.
FAQs – Pediatric Geneticist & Genetic Testing in Children
A pediatric geneticist is a pediatrician with specialized training in diagnosing, treating, and managing genetic disorders in children. These disorders include chromosomal abnormalities, birth defects, inherited metabolic disorders, and delays in development. Pediatric geneticists also offer genetic counseling to families and collaborate with other specialists, including neurologists, cardiologists, and endocrinologists.
Yes, to pursue Genetics (as mentioned above) in India, aspirants are required to clear the NEET-UG exam for admission to MBBS (Bachelor of Medicine and Bachelor of Surgery). Following MBBS, one has to do MD/ DNB in Pediatrics/ Internal Medicine and further super-specialization/Fellowship in Medical Genetics.
To be a pediatric geneticist in India, here’s what you should do:
Clear NEET and complete MBBS
Go for MD Pediatrics or its equivalent
Specialize in Medical Genetics through DM (Doctorate of Medicine), fellowship programs, or postdoctoral programs
Obtain clinical experience in pediatric genetic clinics or academia
This training pathway will prepare you to practice as a child genetic physician who diagnoses and manages complex inherited diseases.
Yes, a medical geneticist is a board-certified physician. Both have an MBBS and further expertise in genetics. They usually work in a clinical capacity, diagnosing hereditary conditions, running genetic tests, and planning care for children and families.
There is no direct MD course in Genetics presently in India. But you can do a DM in Medical Genetics after doing an MD in Pediatrics, Internal Medicine, or Obstetrics, such as AIIMS/ SGPGI, etc. Additionally, look into fellowships and research programs in clinical or pediatric genetics.
A pediatric geneticist’s salary level is determined by experience, location, and type of hospital:
Fresher (0 – 3 years): ₹8 – 12 LPA
Mid-level (4-8 years): ₹15-20 LPA
Senior consultants (10+ years): ₹25–35 LPA+
Genetic testing in children can reveal changes in chromosomes, genes, or proteins resulting from an inherited disorder. It includes tests like:
Karyotyping
CGH Array
Whole Exome Sequencing
Newborn screening
The testing can help diagnose autism, Down syndrome, metabolic conditions, and more. It is non- or minimally invasive, for example, requiring only a blood sample or a buccal swab.
Prices of Genetic tests in Bangalore greatly vary between ₹5,000 and ₹50,000 and more , depending on the test, plus a consultation fee. For example:
Karyotyping: ₹5,000–₹8,000
CGH Array: ₹15,000–₹20,000
Whole Exome Sequencing: ₹30,000–₹50,000 +
Make sure to discuss and clinically consult with a pediatric genetics doctor in Bangalore to determine which of these tests is suitable for your child.
A medical geneticist or pediatric geneticist is a physician who orders and interprets genetic testing for children. They learn to identify signs of inherited conditions, recommend relevant tests, and create tailored care plans.
Conditions treated by pediatric geneticists can be extensive and include:
Physical deformities (e.g., cleft lip or heart abnormalities)
Syndromes (such as Down syndrome or Marfan’s syndrome) that are inherited through genes
Metabolic conditions (such as cystic fibrosis, PKU)
Delays in developmental and autism
Genetic factors (such as hemophilia, muscular dystrophy)
They, too, offer families genetic counseling and lifelong multi-disciplinary care.
Yes, it is safe for children to be genetically tested. Most are taken via a routine blood sample or gel swab of saliva. Invasive procedures, such as biopsies, are seldom necessary. The tests are administered under clinical supervision, and the risks are minimal.
You can find one at:
Manipal Hospital, Old Airport Road: This is still at an initial stage, but here you go!
You can visit: Rainbow Children’s Hospital, Hebbal & Marathahalli
Aster CMI, Hebbal
Apollo Hospitals, Bannerghatta & Jayanagar. It is a highly sanitized and clean hospital.
Baptist Hospital, Hebbal
Consult a Pediatric Genetics Doctor in Bangalore Today
Sometimes, an early diagnosis is all the difference in treating genetic disorders in children. Whether you’re worried about a family history of inherited conditions or your child’s developmental delays, seeing a pediatric genetics doctor in Bangalore provides timely, accurate, and empathetic assistance. Our experts offer tailored treatment protocols, pioneering genetic testing, and family-centered guidance to assist you throughout the process.